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Qualis LIMS

Optimizes and manages laboratory processes for various industries, ensuring compliance, traceability, and comprehensive reporting.

Overview

Qualis LIMS is a configurable Laboratory Information Management System that facilitates paperless management of all laboratory processes, covering everything from sample receipt to report generation. It is designed to be industry agnostic, making it suitable for Quality Control (QC), research, healthcare, and commercial labs.

Qualis LIMS offers integrated modules to document laboratory investigations and results while adhering to regulatory compliance standards. Its capabilities include tracking Key Performance Indicators (KPIs), receiving alerts for approvals, calibration dates, and job statuses, as well as recording test results and generating reports through its built-in reporting tool.

Dynamic Sample Registration

Users can design input templates with a drag-and-drop interface for dynamic sample registration, allowing the management of various sample types such as raw materials and patient samples. These templates help in maintaining traceability throughout the sample lifecycle and can be validated, approved, and modified with version and release control.

Laboratory Efficiency and Compliance

Qualis LIMS supports sample pre-registration, manual and instrument-interface result entry, and sample approvals and releases by relevant authorities. It offers features like test and specification management, job allocation to certified personnel and instruments, and standardized inventory management with barcode labeling.

Comprehensive Reporting and Inventory

The system includes designing report templates with an auto-generated SQL Query Builder and supports electronic signatures for quick report approval and release. Additionally, it manages instrument usage and logs, ensuring only calibrated instruments are used for tests.

Key Benefits

  • Fully web-based, accessible via standard browsers.
  • Highly scalable, supporting multi-site, multi-department configurations.
  • Compliance with 21 CFR Part 11 / EudraLex Annex 11 standards ensures high reliability and low compliance costs.
  • No-code configurable platform for easy setup and rapid validation.

This robust system empowers laboratories beyond basic management, emphasizing efficiency, regulatory compliance, and growth potential.

Meta

Category
Laboratory Information Management System (LIMS)
Field(s)
Lab OperationsQuality & Compliance
Target user(s)
Lab Manager / Core Facility ManagerQA / Regulatory Affairs
Tag(s)
Quality & Compliance Management